Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth

American Journal of Medical Genetics

Volumn 75, Issue 1, 1998, Pages 13-17

  Innis, Jeffrey W ^a   Sieving, Paul A ^b   McMillan, Pamella ^b   Weatherly, Robert A ^b  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Autosomal recessive; Delay in tooth eruption; Discolored enamel; Retinal pigment epithelium; Sensorineural hearing loss

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CHILD; CLINICAL FEATURE; FEMALE; HUMAN; MALE; PEDIGREE; PERCEPTION DEAFNESS; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINA PIGMENT EPITHELIOPATHY; SYNDROME DELINEATION; TOOTH COLOR;

CHILD, PRESCHOOL; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; PEDIGREE; PIGMENT EPITHELIUM OF EYE; SYNDROME; TOOTH DISCOLORATION; TOOTH ERUPTION, ECTOPIC;

EID: 0031974523     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980106)75:1<13::AID-AJMG4>3.0.CO;2-R     Document Type: Article

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